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PROK2 Protein (Transcript Variant 2)

Cette protéine Recombinant PROK2 est exprimée dans Escherichia coli (E. coli).
N° du produit ABIN2729731

Aperçu rapide pour PROK2 Protein (Transcript Variant 2) (ABIN2729731)

Antigène

Voir toutes PROK2 Protéines
PROK2 (Prokineticin 2 (PROK2))

Type de proteíne

Recombinant

Origine

  • 5
  • 3
  • 3
  • 2
Humain

Source

  • 10
  • 2
  • 1
Escherichia coli (E. coli)

Application

Antibody Production (AbP), Standard (STD)

Pureté

> 95 % as determined by SDS-PAGE and Coomassie blue staining
  • Attributs du protein

    Transcript Variant 2

    Attributs du produit

    • Recombinant human PROK2 / PK2 (transcript variant 2) protein expressed in E. coli.
    • Produced with end-sequenced ORF clone

    niveau d'endotoxine

    Endotoxin level is <0.1 ng/μg of protein (<1EU/μg).
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  • Indications d'application

    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays

    Restrictions

    For Research Use only
  • Buffer

    Lyophilized from a 0.2 μM filtered solution of 20 mM phosphate buffer,100 mM NaCl, pH 7.2

    Conseil sur la manipulation

    Resuspend the protein in the desired concentration in proper buffer

    Stock

    -80 °C

    Stockage commentaire

    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Antigène

    PROK2 (Prokineticin 2 (PROK2))

    Autre désignation

    Prok2,pk2

    Sujet

    This gene encodes a protein expressed in the suprachiasmatic nucleus (SCN) circadian clock that may function as the output component of the circadian clock. The secreted form of the encoded protein may also serve as a chemoattractant for neuronal precursor cells in the olfactory bulb. Proteins from other vertebrates which are similar to this gene product were isolated based on homology to snake venom and secretions from frog skin, and have been shown to have diverse functions. Mutations in this gene are associated with Kallmann syndrome 4. Multiple transcript variants encoding different isoforms have been found for this gene.

    Poids moléculaire

    8.8 kDa

    NCBI Accession

    NP_068754
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